Regulations from several entities guide the management of your grant. If you have any questions about regulations and how they apply to your grant, contact your grantee organization.
- Ahrens, T. (2005). Evidenced-based practice: Priorities and implementation strategies. AACN Advanced Critical Care, 16(1), 36-42.
- Cook, D. (1998). Evidence-based critical care medicine: A potential tool for change.New Horizon, 6(1), 20-25.
- Kelley, P. (2002). Research to practice in the military health care system. TSNRP grant N02-P18.
- Nieva, V., Murphy, R., Ridley, N., Donaldson, N., Combers, J., Mitchell, P., et al. (2005). From science to service: A framework for the transfer of patient safety research into practice. In Advances in patient safety: From research to implementation(vol. 2, pp. 441-453). Rockville, MD: Agency for Healthcare Research and Quality.
- Sackett, K. L., Straus, S. E., Richardson, W. S., Rosenberg, W., & Haynes, R. B. (2000). Evidence-based medicine; How to practice and teach EBM. London: Churchill Livingstone.
- Titler, M. G. (2006). Developing and evidence-based practice (6th ed.). St Louis, MO: Mosby, Inc.
Grant Management Regulations
2 Code of Federal Regulations (CFR) Part 215, Uniform Administrative Requirements for Grants and Other Agreements with Institutions of Higher Education, Hospitals and Other Non-Profit Organizations, 19 November 1993, amended 30 September 1999. Formerly known as OMB Circular A-110.
Human Subjects Protection
HA Policy 05-003, Policy for Protection of Human Subjects in DoD Sponsored Research, Health Affairs Under Secretary of Defense for Personnel and Readiness, 28 Mar 2005.
Title 21 Code of Federal Regulations (CFR) 50, Protection of Human Subjects.
Title 21 Code of Federal Regulations (CFR) 56, Institutional Review Boards.
Title 21 Code of Federal Regulations (CFR) 312, Investigational New Drug Application.
Title 21 Code of Federal Regulations (CFR) 812, Food and Drugs Chapter I: Food and Drug Administration Department of Health and Human Services, Subchapter H: Medical Devices, Part 812. Investigational Device Exemptions.
Title 21 Code of Federal Regulations (CFR) 600, Biological Products, General.
Title 21 Code of Federal Regulations (CFR) 314, Applications for FDA Approval to Market a New Drug.
Title 32 CFR 219, Human Subjects Protection.
Title 45 CFR 46, Subparts A, B, C, and D, Protection of Human Subjects.
Title 24 U.S. Code 30, Payment to Donors of Blood for Persons Undergoing Treatment at Government Expense.
U.S. Army Regulations
AR 40-38, Clinical Investigation Programs, 1 September 1989.
AR 70-25, Use of Volunteers as Subjects of Research, 25 January 1990.
U. S. Navy Regulations
Summary of Significant Changes SECNAVINST 3900.39C to 3900.39D, 22 June 2007.
Non-Human Animal Subjects
Title Code of Federal Regulations (CFR) Subpart A-D, Animals and Animal Products.
American Veterinary Medical Association (AVMA), AVMA Guidelines on Euthanasia, June 2007.
USUHSINST 3203, The Care and Use of Laboratory Animals in DoD Programs, incorporates Army Regulation 40-33, SECNAVINST 3900.38, AFMAN 40-401(1), and DARPAINST 18 (Defense Advanced Research Projects Agency Instruction).
Title 45 Code of Federal Regulations (CFR) 689, Research Misconduct.